Join Our Team at Techfirm Industrie AG!
Techfirm Industrie AG is seeking dedicated support to enhance our operations in Wallis, specifically within the pharmaceutical production area. We are currently looking for a colleague to take on Batch Record Reviewing activities. If you are interested in contributing to a dynamic and professional environment, we encourage you to explore this opportunity!
Main Purpose of This Role
The primary responsibility of this role is to ensure that each batch is produced in accordance with established procedures and regulatory requirements. Successful reviewers display exceptional attention to detail, the ability to work independently, and possess in-depth knowledge of the manufacturing processes they are reviewing.
What You'll Do
- Conduct thorough reviews of Executed Batch Records, including production documentation and raw data.
- Support batch release by ensuring the completeness of the documentation package.
- Review comments added to the Executed Batch Records, clarify with the operations team, and evaluate findings with the responsible QA Manager.
- Assist in the initiation of deviations and investigations related to Batch Record review observations.
What We’re Looking For
- An academic degree or relevant work experience in Biology, Chemistry, Biotechnology, or a related field.
- Previous experience in a GMP-regulated pharmaceutical or API industry is preferred.
- The ability to identify non-compliance and gaps in quality standards.
- A structured, precise, and well-organized working attitude, with an openness to new ideas and a dynamic drive.
- Fluency in English (both written and verbal) is required, with German language skills being an advantage.
Apply online using the form below. Please note that only applications matching the job profile will be considered.
Work locationVisp, Switzerland